Canonical Allele Identifier: CA349411839

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396952T>C (hg19) ; chr2:g.178532225T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532225T>C , CM000664.2:g.178532225T>C	GRCh38
NC_000002.11:g.179396952T>C , CM000664.1:g.179396952T>C	GRCh37
NC_000002.10:g.179105198T>C	NCBI36
NG_011618.3:g.303578A>G , LRG_391:g.303578A>G
NG_051363.1:g.14399T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96686A>G (TTN)	ENSP00000343764.6:p.Glu32229Gly
ENST00000342175.11:c.77771A>G (TTN)	ENSP00000340554.6:p.Glu25924Gly
ENST00000359218.10:c.77570A>G (TTN)	ENSP00000352154.5:p.Glu25857Gly
ENST00000342175.10:c.77771A>G (TTN)	ENSP00000340554.6:p.Glu25924Gly
ENST00000342992.10:c.96686A>G (TTN)	ENSP00000343764.6:p.Glu32229Gly
ENST00000359218.9:c.77570A>G (TTN)	ENSP00000352154.5:p.Glu25857Gly
ENST00000460472.6:c.77195A>G (TTN)	ENSP00000434586.1:p.Glu25732Gly
ENST00000589042.5:c.104390A>G (TTN) MANE Select	ENSP00000467141.1:p.Glu34797Gly
ENST00000591111.5:c.99467A>G (TTN)	ENSP00000465570.1:p.Glu33156Gly
ENST00000615779.4:c.99467A>G (TTN)	ENSP00000483597.1:p.Glu33156Gly
NM_001256850.1:c.99467A>G (TTN)	NP_001243779.1:p.Glu33156Gly
NM_001267550.2:c.104390A>G (TTN) MANE Select	NP_001254479.2:p.Glu34797Gly
NM_003319.4:c.77195A>G (TTN)	NP_003310.4:p.Glu25732Gly
NM_133378.4:c.96686A>G (TTN)	NP_596869.4:p.Glu32229Gly
NM_133432.3:c.77570A>G (TTN)	NP_597676.3:p.Glu25857Gly
NM_133437.4:c.77771A>G (TTN)	NP_597681.4:p.Glu25924Gly
NR_038271.1:n.446+8589T>C (TTN-AS1)
NR_038272.1:n.220-3507T>C (TTN-AS1)
XM_011511729.1:c.103487A>G (TTN)	XP_011510031.1:p.Glu34496Gly
XM_011511730.1:c.77381A>G (TTN)	XP_011510032.1:p.Glu25794Gly
XM_011511731.1:c.77240A>G (TTN)	XP_011510033.1:p.Glu25747Gly
XM_017004819.1:c.103283A>G (TTN)	XP_016860308.1:p.Glu34428Gly
XM_017004820.1:c.98681A>G (TTN)	XP_016860309.1:p.Glu32894Gly
XM_017004821.1:c.98678A>G (TTN)	XP_016860310.1:p.Glu32893Gly
XM_017004822.1:c.95720A>G (TTN)	XP_016860311.1:p.Glu31907Gly
XM_017004823.1:c.77336A>G (TTN)	XP_016860312.1:p.Glu25779Gly
XM_024453094.1:c.98831A>G (TTN)	XP_024308862.1:p.Glu32944Gly
XM_024453095.1:c.98828A>G (TTN)	XP_024308863.1:p.Glu32943Gly
XM_024453096.1:c.98261A>G (TTN)	XP_024308864.1:p.Glu32754Gly
XM_024453097.1:c.95603A>G (TTN)	XP_024308865.1:p.Glu31868Gly
XM_024453098.1:c.95522A>G (TTN)	XP_024308866.1:p.Glu31841Gly
XM_024453099.1:c.77285A>G (TTN)	XP_024308867.1:p.Glu25762Gly
XM_024453100.1:c.67139A>G (TTN)	XP_024308868.1:p.Glu22380Gly